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Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons
Dopamine neurons have different synaptic actions in the ventral and dorsal striatum (dStr), but whether this heterogeneity extends to dStr subregions has not been addressed. We have found that optogenetic activation of dStr dopamine neuron terminals in mouse brain slices pauses the firing of choline...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175576/ https://www.ncbi.nlm.nih.gov/pubmed/30295607 http://dx.doi.org/10.7554/eLife.39786 |
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author | Chuhma, Nao Mingote, Susana Yetnikoff, Leora Kalmbach, Abigail Ma, Thong Ztaou, Samira Sienna, Anna-Claire Tepler, Sophia Poulin, Jean-Francois Ansorge, Mark Awatramani, Rajeshwar Kang, Un Jung Rayport, Stephen |
author_facet | Chuhma, Nao Mingote, Susana Yetnikoff, Leora Kalmbach, Abigail Ma, Thong Ztaou, Samira Sienna, Anna-Claire Tepler, Sophia Poulin, Jean-Francois Ansorge, Mark Awatramani, Rajeshwar Kang, Un Jung Rayport, Stephen |
author_sort | Chuhma, Nao |
collection | PubMed |
description | Dopamine neurons have different synaptic actions in the ventral and dorsal striatum (dStr), but whether this heterogeneity extends to dStr subregions has not been addressed. We have found that optogenetic activation of dStr dopamine neuron terminals in mouse brain slices pauses the firing of cholinergic interneurons in both the medial and lateral subregions, while in the lateral subregion the pause is shorter due to a subsequent excitation. This excitation is mediated mainly by metabotropic glutamate receptor 1 (mGluR1) and partially by dopamine D1-like receptors coupled to transient receptor potential channel 3 and 7. DA neurons do not signal to spiny projection neurons in the medial dStr, while they elicit ionotropic glutamate responses in the lateral dStr. The DA neurons mediating these excitatory signals are in the substantia nigra (SN). Thus, SN dopamine neurons engage different receptors in different postsynaptic neurons in different dStr subregions to convey strikingly different signals. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). |
format | Online Article Text |
id | pubmed-6175576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61755762018-10-17 Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons Chuhma, Nao Mingote, Susana Yetnikoff, Leora Kalmbach, Abigail Ma, Thong Ztaou, Samira Sienna, Anna-Claire Tepler, Sophia Poulin, Jean-Francois Ansorge, Mark Awatramani, Rajeshwar Kang, Un Jung Rayport, Stephen eLife Neuroscience Dopamine neurons have different synaptic actions in the ventral and dorsal striatum (dStr), but whether this heterogeneity extends to dStr subregions has not been addressed. We have found that optogenetic activation of dStr dopamine neuron terminals in mouse brain slices pauses the firing of cholinergic interneurons in both the medial and lateral subregions, while in the lateral subregion the pause is shorter due to a subsequent excitation. This excitation is mediated mainly by metabotropic glutamate receptor 1 (mGluR1) and partially by dopamine D1-like receptors coupled to transient receptor potential channel 3 and 7. DA neurons do not signal to spiny projection neurons in the medial dStr, while they elicit ionotropic glutamate responses in the lateral dStr. The DA neurons mediating these excitatory signals are in the substantia nigra (SN). Thus, SN dopamine neurons engage different receptors in different postsynaptic neurons in different dStr subregions to convey strikingly different signals. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). eLife Sciences Publications, Ltd 2018-10-08 /pmc/articles/PMC6175576/ /pubmed/30295607 http://dx.doi.org/10.7554/eLife.39786 Text en © 2018, Chuhma et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Chuhma, Nao Mingote, Susana Yetnikoff, Leora Kalmbach, Abigail Ma, Thong Ztaou, Samira Sienna, Anna-Claire Tepler, Sophia Poulin, Jean-Francois Ansorge, Mark Awatramani, Rajeshwar Kang, Un Jung Rayport, Stephen Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
title | Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
title_full | Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
title_fullStr | Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
title_full_unstemmed | Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
title_short | Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
title_sort | dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175576/ https://www.ncbi.nlm.nih.gov/pubmed/30295607 http://dx.doi.org/10.7554/eLife.39786 |
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